125 related articles for article (PubMed ID: 25047868)
1. Computational and ¹³C investigations of the diazadienes and oxazadienes formed via the rearrangement of methylenecyclopropyl hydrazones and oximes.
Chen B; Scott ME; Adams BA; Hrovat DA; Borden WT; Lautens M
Org Lett; 2014 Aug; 16(15):3930-3. PubMed ID: 25047868
[TBL] [Abstract][Full Text] [Related]
2. Synthesis of pyrroles through a 4π-electrocyclic ring-closure reaction of 1-azapentadienyl cations.
Narayan R; Fröhlich R; Würthwein EU
J Org Chem; 2012 Feb; 77(4):1868-79. PubMed ID: 22296045
[TBL] [Abstract][Full Text] [Related]
3. A highly efficient and selective route to isomeric cyclic diazadienes.
Scott ME; Bethuel Y; Lautens M
J Am Chem Soc; 2007 Feb; 129(6):1482-3. PubMed ID: 17283979
[No Abstract] [Full Text] [Related]
4. Regioselective synthesis of 2,3,4- or 2,3,5-trisubstituted pyrroles via [3,3] or [1,3] rearrangements of O-vinyl oximes.
Wang HY; Mueller DS; Sachwani RM; Kapadia R; Londino HN; Anderson LL
J Org Chem; 2011 May; 76(9):3203-21. PubMed ID: 21449572
[TBL] [Abstract][Full Text] [Related]
5. Expedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethers.
Jiang Y; Chan WC; Park CM
J Am Chem Soc; 2012 Mar; 134(9):4104-7. PubMed ID: 22332783
[TBL] [Abstract][Full Text] [Related]
6. Carbon-carbon bond formation and pyrrole synthesis via the [3,3] sigmatropic rearrangement of O-vinyl oxime ethers.
Wang HY; Mueller DS; Sachwani RM; Londino HN; Anderson LL
Org Lett; 2010 May; 12(10):2290-3. PubMed ID: 20411970
[TBL] [Abstract][Full Text] [Related]
7. Investigation on the Beckmann rearrangement reaction catalyzed by porous solids: MAS NMR and theoretical calculations.
Lezcano-González I; Boronat M; Blasco T
Solid State Nucl Magn Reson; 2009 Apr; 35(2):120-9. PubMed ID: 19286355
[TBL] [Abstract][Full Text] [Related]
8. Study of conformations and hydrogen bonds in the configurational isomers of pyrrole-2-carbaldehyde oxime by 1H, 13C and 15N NMR spectroscopy combined with MP2 and DFT calculations and NBO analysis.
Afonin AV; Ushakov IA; Pavlov DV; Ivanov AV; Mikhaleva AI
Magn Reson Chem; 2010 Sep; 48(9):685-92. PubMed ID: 20623827
[TBL] [Abstract][Full Text] [Related]
9. Fast alpha nucleophiles: structures that undergo rapid hydrazone/oxime formation at neutral pH.
Kool ET; Crisalli P; Chan KM
Org Lett; 2014 Mar; 16(5):1454-7. PubMed ID: 24559274
[TBL] [Abstract][Full Text] [Related]
10. Synthesis of an enlarged library of dynamic DNA activators with oxime, disulfide and hydrazone bridges.
Montenegro J; Bang EK; Sakai N; Matile S
Chemistry; 2012 Aug; 18(33):10436-43. PubMed ID: 22589231
[TBL] [Abstract][Full Text] [Related]
11. Pronounced stereospecificity of (1)H, (13)C, (15)N and (77)Se shielding constants in the selenophenyl oximes as shown by NMR spectroscopy and GIAO calculations.
Afonin AV; Pavlov DV; Ushakov IA; Schmidt EY; Mikhaleva AI
Magn Reson Chem; 2009 Oct; 47(10):879-84. PubMed ID: 19582802
[TBL] [Abstract][Full Text] [Related]
12. Molecular structure, heteronuclear resonance assisted hydrogen bond analysis, chemical reactivity and first hyperpolarizability of a novel ethyl-4-{[(2,4-dinitrophenyl)-hydrazono]-ethyl}-3,5-dimethyl-1H-pyrrole-2-carboxylate: a combined DFT and AIM approach.
Singh RN; Kumar A; Tiwari RK; Rawat P; Baboo V; Verma D
Spectrochim Acta A Mol Biomol Spectrosc; 2012 Jun; 92():295-304. PubMed ID: 22446779
[TBL] [Abstract][Full Text] [Related]
13. A general modular method of azaindole and thienopyrrole synthesis via Pd-catalyzed tandem couplings of gem-dichloroolefins.
Fang YQ; Yuen J; Lautens M
J Org Chem; 2007 Jul; 72(14):5152-60. PubMed ID: 17559273
[TBL] [Abstract][Full Text] [Related]
14. Fragmentation of oxime and silyl oxime ether odd-electron positive ions by the McLafferty rearrangement: new insights on structural factors that promote α,β fragmentation.
Laulhé S; Bogdanov B; Johannes LM; Gutierrez O; Harrison JG; Tantillo DJ; Zhang X; Nantz MH
J Mass Spectrom; 2012 Jun; 47(6):676-86. PubMed ID: 22678949
[TBL] [Abstract][Full Text] [Related]
15. Optoelectronic tuning of organoborylazadipyrromethenes via effective electronegativity at the metalloid center.
Berhe SA; Rodriguez MT; Park E; Nesterov VN; Pan H; Youngblood WJ
Inorg Chem; 2014 Mar; 53(5):2346-8. PubMed ID: 24533769
[TBL] [Abstract][Full Text] [Related]
16. Vibrational frequency analysis, FT-IR, FT-Raman, ab initio, HF and DFT studies, NBO, HOMO-LUMO and electronic structure calculations on pycolinaldehyde oxime.
Suvitha A; Periandy S; Boomadevi S; Govindarajan M
Spectrochim Acta A Mol Biomol Spectrosc; 2014 Jan; 117():216-24. PubMed ID: 23994677
[TBL] [Abstract][Full Text] [Related]
17. Gold-catalysed rearrangement of O-vinyl oximes for the synthesis of highly substituted pyrroles.
Ngwerume S; Camp JE
Chem Commun (Camb); 2011 Feb; 47(6):1857-9. PubMed ID: 21132178
[TBL] [Abstract][Full Text] [Related]
18. [Reactions of N-quaternary 1-phenyl-3,4-dihydroisoquinolinium compounds with nucleophiles--products and their isomerism--part 2].
Möhrle H; Breves H
Pharmazie; 2005 Jan; 60(1):23-35. PubMed ID: 15700775
[TBL] [Abstract][Full Text] [Related]
19. Study of the Beckmann rearrangement of acetophenone oxime over porous solids by means of solid state NMR spectroscopy.
Fernandez AB; Lezcano-Gonzalez I; Boronat M; Blasco T; Corma A
Phys Chem Chem Phys; 2009 Jul; 11(25):5134-41. PubMed ID: 19562146
[TBL] [Abstract][Full Text] [Related]
20. Water-soluble organocatalysts for hydrazone and oxime formation.
Crisalli P; Kool ET
J Org Chem; 2013 Feb; 78(3):1184-9. PubMed ID: 23289546
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]